146763-62-4Relevant articles and documents
Total synthesis of gambierol by using oxiranyl anions
Furuta, Hiroki,Hasegawa, Yuki,Hase, Mariko,Mori, Yuji
supporting information; experimental part, p. 7586 - 7595 (2010/09/11)
Gambierol was isolated as a neurotoxin from the cultured cells of the ciguatera causative dinoflagellate Gambierdiscus toxicus and classified as a member of the polycyclic ether family of marine toxins. The structure consists of a ladder-shaped frans-fuse
Total synthesis of gambierol
Furuta, Hiroki,Hasegawa, Yuki,Mori, Yuji
supporting information; experimental part, p. 4382 - 4385 (2009/12/26)
The total synthesis of gambierol has been achieved utilizing an oxiranyl anion strategy in an iterative manner. Synthetic highlights of this route include direct carbon-carbon formation on epoxides, sulfonyl-assisted 6-endo cyclization, and expansion reac
Diverted total synthesis and biological evaluation of gambierol analogues: Elucidation of crucial structural elements for potent toxicity
Fuwa, Haruhiko,Kainuma, Noriko,Tachibana, Kazuo,Tsukano, Chihiro,Satake, Masayuki,Sasaki, Makoto
, p. 4894 - 4909 (2007/10/03)
Gambierol is a polycyclic ether toxin, which has been isolated from the marine dinoflagellate Gambierdiscus toxicus. A series of gambierol analogues have been prepared from an advanced intermediate of our total synthesis of gambierol and investigated for